ProRx recalls Semag: 12.5/5mL (2.5 mg/mL) multidose vials due to lack of sterility assurance. Affected units have NDC 84139-225-09 and lot number Prorx04282025-3. Stop using immediately.
Lack of Assurance of Sterility
ProRx is recalling Semaglutide injections that may not be sterile, which could cause infections. This is a serious risk for people using the medication as prescribed.
The vials lack proper sterility assurance, meaning they could become contaminated with bacteria. If injected, this could lead to serious infections or even life-threatening conditions.
People with prescriptions for Semaglutide injections from ProRx are affected. Those using the product for weight loss or diabetes treatment are at highest risk.
Check for the NDC code 84139-225-09 and lot number Prorx04282025-3 on the vial label. The product is a 5mL multidose vial for subcutaneous use.
Discard all affected vials to prevent potential infection from contaminated medication.
No, the product has a lack of sterility assurance, which could cause infections. Do not use.
The NDC number is 84139-225-09.
Look for the NDC code 84139-225-09 and lot number Prorx04282025-3 on the vial label.
We’ve drafted a message you can send ProRx to request your refund or repair — edit it as you like.
Subject: Recall D-0114-2026 — ProRx ProRx Hello, I own a ProRx that is covered by recall D-0114-2026 from ProRx. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
